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American Pharmaceutical News In Review
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July 21, 2022
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  Manufacturing Aseptically Filled Drugs and Biopharmaceuticals Starts with a Sound Sterility Assurance Program

As an emerging pharmaceutical company, making sure that your product is tested and sterilized appropriately is essential. Some important things you must consider are contamination control, environmental monitoring, aseptic processing, container-closure integrity, and E&L testing. You can learn about these challenges directly from our industry experts in Philadelphia October 26th & 27th.

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» Industry News
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  Envigo Agrees with US Department of Justice and Department of Agriculture to Resolve Complaints
Inotiv, announced that Envigo entered a settlement with the US Department of Justice (DOJ) and the ... read more »
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  EMA Validates Marketing Authorization Application for Trastuzumab Duocarmazine in HER2-Positive Metastatic Breast Cancer
Byondis B.V., an independent, Dutch clinical stage biopharmaceutical company, announced that the ... read more »
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  Eton Pharma Receives FDA Approval for Zonisamide Oral Suspension
Eton Pharmaceuticals, Inc. announced that the FDA has approved ZONISADE™ (zonisamide oral suspension... read more »
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  TFF Pharmaceuticals Elevates R&D Operations with New Facility in Austin, Texas
TFF Pharmaceuticals announced an expansion of its R&D operations through the lease of a new research... read more »

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» QC Corner
QC Corner
  QC Corner: Environmental Monitoring as a Component of a Contamination Control Strategy
Watch Now! In this webinar, Mark Hallworth discusses environmental monitoring as a component of a ... read more »

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» Infographic
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  Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Recombinant Horseshoe Crab Factor C (rFC) provides a sustainable, highly effective, and environmentally friendly sustainable means of endotoxin ... read more »
» Featured Articles
Affinity Approaches to Selective, Sensitive MS Assays
Use of antibodies for detection of very low analyte concentrations has been evolving since Yalow and Berson developed the radioimmunoassay in the late... read more »
Method Changes for Bacterial Endotoxins Testing (BET): Steps to Follow for a Straightforward Process
Quality Control departments in the pharmaceutical industry often seek new, innovative products to simplify their testing. They want compliant and ... read more »
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» Featured Video
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  On-Demand Webinar: Powder Rheology and Mechanics
Understand powder rheology to make tableting successful. In this webinar, you’ll learn Powder Rheology, Material Characterization, and USP <1062> Tablet ... watch »
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  On-Demand Webinar: The Data Quality Journey – Focus on Environmental Monitoring Systems
Live Webinar: The Data Quality Journey – Focus on Environmental Monitoring Systems watch »

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» Featured Whitepaper
eBook: Raman Imaging in Pharmaceutical Research
In order to ensure the efficacy and safety of pharmaceutical formulations, their chemical composition needs to be monitored during the entire development and production process. read more »
Whitepaper: Development and Validation of a Versatile and Robust Method for Measuring Residual Plasmid DNA
The clearance of residual plasmid DNA must be verified during lot release testing or process development. This is a regulatory requirement and ensures patient safety and product quality. What is ... read more »

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| Events
EVENT
  Pre-Filled Syringes San Francisco
San Francisco, CA –  09/19/2022
The pre-filled syringes industry is growing at an exponential rate with innovations in parenteral delivery device development to aid self-...
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EVENT
  SAE Media Group’s 2nd Annual Biosensors for Medical Wearables
Boston, MA –  10/24/2022
Advances in development and therapeutic applications of on-body sensors SAE Media Group is proud to present the Biosensors for Medical Wearables ...
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